Nuclear envelope budding enables export of large transcripts in muscle cells
Summary
Nuclear envelope (NE) budding (NEB) has emerged as an alternative route for nuclear export of viral particles that are too large to pass through the nuclear pore complex. Yet the significance of this unconventional export pathway for large endogenous cargoes in mammalian cells has remained largely unexplored. Here, we use a combination of electron and fluorescence microscopy to demonstrate that NEB events occur following myoblast differentiation into myotubes and concomitant with the expre
Content
# Nuclear envelope budding enables export of large transcripts in muscle cells
*Published: 2026 Apr 24*
Nuclear envelope (NE) budding (NEB) has emerged as an alternative route for
nuclear export of viral particles that are too large to pass through the nuclear
pore complex. Yet the significance of this unconventional export pathway for
large endogenous cargoes in mammalian cells has remained largely unexplored.
Here, we use a combination of electron and fluorescence microscopy to
demonstrate that NEB events occur following myoblast differentiation into
myotubes and concomitant with the expression of extremely long muscle-specific
transcripts. We show that NE buds are derived from the inner nuclear membrane,
contain internal vesicles, and are specifically enriched with long sarcomeric
transcripts. We identify a role for the protein UAP56-interacting factor (UIF)
in regulating mRNA cargo targeting into NE buds and show that this pathway
requires the endosomal sorting complex required transport III (ESCRT-III)
membrane remodeling machinery. Our findings uncover a non-canonical pathway for
large transcript nuclear export in muscle cells and provide insight into its
mechanism.
DOI: 10.1016/j.cell.2026.03.050